SLC7A9 anticorps
-
- Antigène Voir toutes SLC7A9 Anticorps
- SLC7A9 (Solute Carrier Family 7 (Cationic Amino Acid Transporter, Y+ System), Member 9 (SLC7A9))
-
Reactivité
- Humain, Souris
-
Hôte
- Lapin
-
Clonalité
- Polyclonal
-
Conjugué
- Cet anticorp SLC7A9 est non-conjugé
-
Application
- Western Blotting (WB)
- Purification
- Affinity purification
- Immunogène
- Recombinant protein of human SLC7A9
- Isotype
- IgG
- Top Product
- Discover our top product SLC7A9 Anticorps primaire
-
-
- Indications d'application
- WB 1:500 - 1:1000
- Commentaires
-
Expressed in the brush border membrane in the kidney (at protein level), Kidney, small intestine, liver and placenta
- Restrictions
- For Research Use only
-
- Buffer
- PBS with 0.02 % sodium azide, 50 % glycerol, pH 7.3.
- Agent conservateur
- Sodium azide
- Précaution d'utilisation
- This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
- Stock
- -20 °C
- Stockage commentaire
- Store at -20C. Avoid freeze / thaw cycles.
-
- Antigène
- SLC7A9 (Solute Carrier Family 7 (Cationic Amino Acid Transporter, Y+ System), Member 9 (SLC7A9))
- Autre désignation
- SLC7A9 (SLC7A9 Produits)
- Synonymes
- anticorps BAT1, anticorps CSNU3, anticorps 4F2-LC6, anticorps solute carrier family 7 member 9, anticorps solute carrier family 7 (amino acid transporter light chain, bo,+ system), member 9, anticorps solute carrier family 7 (amino acid transporter light chain, bo,+ system), member 9 L homeolog, anticorps solute carrier family 7 (cationic amino acid transporter, y+ system), member 9, anticorps SLC7A9, anticorps slc7a9, anticorps slc7a9.L, anticorps Slc7a9
- Sujet
- This gene encodes a protein that belongs to a family of light subunits of amino acid transporters. This protein plays a role in the high-affinity and sodium-independent transport of cystine and neutral and dibasic amino acids, and appears to function in the reabsorption of cystine in the kidney tubule. Mutations in this gene cause non-type I cystinuria, a disease that leads to cystine stones in the urinary system due to impaired transport of cystine and dibasic amino acids. Alternate transcript variants, which encode the same protein, have been found for this gene.
- Poids moléculaire
- 53.481 kDa
- ID gène
- 11136
- UniProt
- P82251
-